Success Metrics

Clinical Success Rate
73.3%

Based on 11 completed trials

Completion Rate
73%(11/15)
Active Trials
0(0%)
Results Posted
36%(4 trials)
Terminated
4(25%)

Phase Distribution

Ph phase_4
8
50%
Ph phase_2
3
19%
Ph phase_1
1
6%
Ph phase_3
3
19%
Ph early_phase_1
1
6%

Phase Distribution

2

Early Stage

3

Mid Stage

11

Late Stage

Phase Distribution16 total trials
Early Phase 1First-in-human
1(6.3%)
Phase 1Safety & dosage
1(6.3%)
Phase 2Efficacy & side effects
3(18.8%)
Phase 3Large-scale testing
3(18.8%)
Phase 4Post-market surveillance
8(50.0%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

73.3%

11 of 15 finished

Non-Completion Rate

26.7%

4 ended early

Currently Active

0

trials recruiting

Total Trials

16

all time

Status Distribution
Completed(11)
Terminated(4)
Other(1)

Detailed Status

Completed11
Terminated4
unknown1

Development Timeline

Analytics

Development Status

Total Trials
16
Active
0
Success Rate
73.3%
Most Advanced
Phase 4

Trials by Phase

Early Phase 11 (6.3%)
Phase 11 (6.3%)
Phase 23 (18.8%)
Phase 33 (18.8%)
Phase 48 (50.0%)

Trials by Status

completed1169%
terminated425%
unknown16%

Recent Activity

Clinical Trials (16)

Showing 16 of 16 trials
NCT00991510Phase 4

Comparative Bioavailability of Myfenax® and CellCept® in Kidney Transplant Patients

Terminated
NCT00121784Phase 4

Heart Spare the Nephron (STN) Study - A Study of CellCept (Mycophenolate Mofetil) and Rapamune (Sirolimus) in Heart Transplant Recipients

Terminated
NCT00048152Phase 3

A Study to Assess Use of Zenapax (Daclizumab) and CellCept (Mycophenolate Mofetil) to Improve Kidney Function in Kidney Transplant Patients

Completed
NCT00324506Phase 2

Safety and Efficacy of Cellcept and Avonex as Combination Treatment in Multiple Sclerosis

Completed
NCT00223301Phase 2

Safety Study of Combination Therapy With Intramuscular Avonex and Oral Cellcept in Patients With Multiple Sclerosis

Completed
NCT00433953Phase 1

Genetic Drug Study of Mycophenolic Acid (CellCept) in Pediatric Kidney Transplant Patients

Terminated
NCT00618527Early Phase 1

Combination Therapy Using Cellcept and Rebif in RRMS

Completed
NCT00337493Phase 4

Pharmacogenetic Study of CellCept (Mycophenolate Mofetil) in Kidney Transplant Patients.

Completed
NCT00817687Phase 4

A Study of the Impact of an Early Biopsy in Patients Treated With CellCept (Mycophenolate Mofetil) After Kidney Transplantation

Completed
NCT00121810Phase 4

Kidney Spare the Nephron (STN) Study - A Study of CellCept (Mycophenolate Mofetil) and Rapamune (Sirolimus) in Kidney Transplant Recipients

Completed
NCT00118742Phase 4

Liver Spare the Nephron (STN) Study - A Study of CellCept (Mycophenolate Mofetil) and Sirolimus in Recipients of a Liver Transplant

Completed
NCT00446459Phase 2

Effects of Mycophenolate Mofetil (MMF) On Anti-HLA (Human Leukocyte Antigen)Antibody Levels In Patients Awaiting Cadaveric Renal Transplant.

Completed
NCT00737659Phase 4

CellCept® Dose Adjustment Versus Fixed Dose (Standard Care) in Renal Transplant Recipients

Unknown
NCT00683969Phase 3

A Study to Assess the Effect of CellCept (Mycophenolate Mofetil) and Reduced Corticosteroids in Controlling Symptoms of Myasthenia Gravis

Completed
NCT00408213Phase 3

A Continuation Study to Assess the Effect of CellCept in Patients With Myasthenia Gravis.

Completed
NCT00420472Phase 4

A Study of CellCept (Mycophenolate Mofetil) in Kidney Transplant Patients Switched From EC-MPS.

Terminated

All 16 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
16